The invention relates to novel substituted bipiperidinyl derivatives, to processes for their preparation, to their use for the treatment and/or prevention of diseases and to their use for preparing medicaments for the treatment and/or prevention of diseases, in particular for the treatment and/or prevention of diabetic microangiopathies, diabetic ulcers on the extremities, in particular for promoting wound healing of diabetic foot ulcers, diabetic heart failure, diabetic coronary microvascular heart disorders, peripheral and cardiac vascular disorders, thromboembolic disorders and ischaemias, peripheral circulatory disturbances, Raynaud's phenomenon, CREST syndrome, microcirculatory disturbances, intermittent claudication, and peripheral and autonomous neuropathies.
COMPOUNDS THAT ARE AGONISTS OF MUSCARINIC RECEPTORS AND THAT MAY BE EFFECTIVE IN TREATING PAIN, ALZHEIMER'S DECEASE AND/OR SCHIZOPHRENIA
申请人:AstraZeneca AB
公开号:EP2024359A1
公开(公告)日:2009-02-18
SUBSTITUIERTE BIPIPERIDINYL-DERIVATE ALS ADRENOREZEPTOR ALPHA 2C ANTAGONISTEN
申请人:Bayer Pharma Aktiengesellschaft
公开号:EP3083594A1
公开(公告)日:2016-10-26
PYRIMIDINE, PYRIDINE AND TRIAZINE DERIVATIVES AS MAXI-K CHANNEL OPENERS
申请人:Tsuzuki Yasuyuki
公开号:US20110034435A1
公开(公告)日:2011-02-10
A compound of formula (A); wherein ring A is an aromatic ring or a heteroaromatic ring; R
1
is independently halogen, cyano, etc., each of X
1
, X
2
and X
3
is CR
2
or nitrogen, R
2
is independently hydrogens, etc., n is 0, 1, 2, 3 or 4; -D-Y is —O—CH
2
COOH, etc, and G is a substituted amino, a substituted heterocyclic group, etc, or a pharmaceutical acceptable salt thereof, has activities of opening BK channels.